Purification method of psoralen and isopsoralen
A technology of isopsoralen and psoralen, which is applied in the field of extraction and purification of traditional Chinese medicine, and can solve the problems of optic nerve damage and inability to operate in practice.
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Embodiment 1
[0019] Take the above-mentioned medicinal solution with a relative density of 0.80-0.98 and dilute it with distilled water (0.01g of crude drug per milliliter of medicinal solution, 20°C), and pass it through a commercially available HPD600 macroporous adsorption resin, and the diameter-to-column ratio after loading the resin is 1:1.1 , pre-adsorption for 3 hours, the flow rate is 6ml / min. Use 20%-30% ethanol 20-30 times the mass of the resin to elute the impurities first. Then use 50%-60% ethanol 6-8 times the mass of the resin to elute the impurities. Collect 50%-60% of the eluate. After recovering the ethanol, concentrate and dry in vacuum to obtain the enriched product of psoralen and isopsoralen. Through the high-performance liquid phase test, the content of psoralen and isopsoralen is 56.5% through the external standard one-point method test.
Embodiment 2
[0021] Take the above-mentioned medicinal solution with a relative density of 0.80-0.98 and dilute it with distilled water (the amount of crude drug per milliliter of the medicinal solution is 0.01g, 20°C), and pass it through the commercially available AB-8 macroporous adsorption resin, and the diameter-to-column ratio after loading the resin is 1 : 2, pre-adsorption for 3 hours, the flow rate is 6ml / min. Use 30% ethanol 30-40 times the resin mass to elute impurities first. Impurities were then eluted with 60% ethanol 7 times the mass of the resin. 60% of the eluate was collected. After recovering the ethanol, concentrate and dry in vacuum to obtain the enriched product of psoralen and isopsoralen. Through the high-performance liquid phase test, the content of psoralen and isopsoralen is 57.8% through the external standard one-point method test.
Embodiment 3
[0023] Take the above-mentioned medicinal solution with a relative density of 0.80-0.98 and dilute it with distilled water (the amount of crude drug per milliliter of medicinal solution is 0.01g, 20°C), and pass it through the commercially available D-101 macroporous adsorption resin, and the diameter-to-column ratio after loading the resin is 1. : 1.5, pre-adsorption for 3 hours, the flow rate is 6ml / min. Use 40% ethanol 30 times the mass of the resin to elute the impurities first. Impurities were then eluted with 60% ethanol 8 times the mass of the resin. 60% of the eluate was collected. After recovering the ethanol, concentrate and dry in vacuum to obtain the enriched product of psoralen and isopsoralen. Through the high-performance liquid phase test, the content of psoralen and isopsoralen is 52.1% through the external standard one-point method test.
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